Journal of Medicinal Chemistry · 1977 · 22 citations · 0 references
MedicineMedicinal ChemistryPharmacologyCancer PharmacologyDrug MetabolismEnzymologyDrug-metabolizing EnzymesEnzyme InhibitionEnzyme Kinetics
Synthesis of a series of alpha-hydroxythiol esters made available, for the first time, product-like molecules that were evaluated as inhibitors of the enzyme glyoxalase I and as potential antitumor agents. All the alpha-hydroxythiol esters tested were competitive inhibitors of the enzyme, albeit weak; however, the relative [I]50 values suggested information about the active site. Antileukemic activity in L1210 lymphoid leukemia indicated no significant activity by these alpha-hydroxythiol esters.